RIKEN Center for Biosystems Dynamics Research, Yokohama 230-0045, Japan.
Institute of Microbial Chemistry (BIKAKEN), Tokyo 141-0021, Japan.
Cold Spring Harb Perspect Biol. 2022 Nov 1;14(11):a041254. doi: 10.1101/cshperspect.a041254.
Autophagy is an intracellular degradation system involving de novo generation of autophagosomes, which function as a transporting vesicle of cytoplasmic components to lysosomes for degradation. Isolation membranes (IMs) or phagophores, the precursor membranes of autophagosomes, require millions of phospholipids to expand and transform into autophagosomes, with the endoplasmic reticulum (ER) being the primary lipid source. Recent advances in structural and biochemical studies of autophagy-related proteins have revealed their lipid transport activities: Atg2 at the interface between IM and ER possesses intermembrane lipid transfer activities, while Atg9 at IM and VMP1 and TMEM41B at ER possess lipid scrambling activities. In this review, we summarize recent advances in the establishment of the lipid transport activities of these proteins and their collaboration mechanisms for lipid transport between the ER and IM, and further discuss how unidirectional lipid transport from the ER to IM occurs during autophagosome formation.
自噬是一种涉及自噬体新生的细胞内降解系统,其功能是作为细胞质成分的运输囊泡运送到溶酶体进行降解。隔离膜(IMs)或吞噬体,是自噬体的前体膜,需要数百万个磷脂来扩展和转化为自噬体,内质网(ER)是主要的脂质来源。自噬相关蛋白的结构和生化研究的最新进展揭示了它们的脂质转运活性:位于 IM 和 ER 之间界面的 Atg2 具有膜间脂质转移活性,而位于 IM 的 Atg9、位于 ER 的 VMP1 和 TMEM41B 具有脂质翻转活性。在这篇综述中,我们总结了这些蛋白的脂质转运活性的最新进展及其在 ER 和 IM 之间脂质转运的协作机制,并进一步讨论了在自噬体形成过程中,ER 向 IM 的单向脂质转运是如何发生的。